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Journal of Clinical Medicine|January 25, 2025
Tyrosine Kinase Inhibitor Therapy Enhances Stem Cells Profile and May Contribute to Survival of Chronic Myeloid Leukemiastem CellsSimone Rocco, Alessandro Maglione, Valentina Schiavo, et al.Tomography (Ann Arbor, Mich.)|December 22, 2022
Accuracy of CT-Guided Core-Needle Biopsy in Diagnosis of Thoracic Lesions Suspicious for Primitive Malignancy of the Lung: A Five-Year Retrospective AnalysisElisa Baratella, Stefano Cernic, Pierluca Minelli, et al.Oncology Reports|December 5, 2006
Constitutive phosphorylation of Janus kinase 2 in the GL15 glioblastoma derived human cell lineMiriam Sciaccaluga, Gian Luigi Gianfranceschi, Simone Rocco, et al.Diagnostic Cytopathology|October 7, 2019
Morphometric analysis of atypical glandular cells correctly classifies normal, reactive, and atypical cells in cervical smearsMarco Vicari, Leo Guidobaldi, Eleonora Perrella, et al.Platelets|February 8, 2022
Refractory immune thrombocytopenia successfully treated with bortezomib in a child with 22q11.2 deletion syndrome, complicated by Evans syndrome and hypogammaglobulinemiaFrancesca Conti, Francesca Gottardi, Mattia Moratti, et al.Prenatal Diagnosis|September 30, 2006
Psychological consequences of prenatal diagnosis in a case of familial Angelman syndromeDaniela Turchetti, Elisabetta Razzaboni, Hila Zomer, et al.Frontiers in Genetics|September 27, 2018
Dealing With BRCA1/2 Unclassified Variants in a Cancer Genetics Clinic: Does Cosegregation Analysis Help?Roberta Zuntini, Simona Ferrari, Elena Bonora, et al.Journal of Medical Genetics|December 30, 2023
Clinical implications of VUS reclassification in a single-centre series from application of ACMG/AMP classification rules specified for BRCA1/2Giovanni Innella, Simona Ferrari, Sara Miccoli, et al.Frontiers in Immunology|November 23, 2020
Case Report: A Case of X-Linked Agammaglobulinemia With High Serum IgE Levels and Allergic RhinitisBianca Cinicola, Andrea Uva, Lucia Leonardi, et al.Journal of Immunology Research|April 29, 2016
Clinical Associations of Biallelic and Monoallelic TNFRSF13B Variants in Italian Primary Antibody Deficiency SyndromesFederica Pulvirenti, Roberta Zuntini, Cinzia Milito, et al.Pageof 9